Full Name
Kristin Gribble

Title
Associate Scientist

Kristin Gribble Headshot
Contact Information
Education
B.A. Biology, magna cum laude, Lawrence University, Appleton, WI, 1994
Ph.D., Biological Oceanography, Massachusetts Institute of Technology/Woods Hole Oceanographic Institution Joint Program, Woods Hole, MA, 2006
MBL Affiliation
Location
Research Area
Lab Website

Our research focuses on the mechanisms and outcomes of phenotypic plasticity in life history, both within and across generations. Plasticity is thought to have evolved to maximize fitness, as it allows rapid response to environmental change without requiring genomic mutation. The controlling molecular mechanisms and adaptive and evolutionary consequences of plasticity are poorly understood, however. We are interested in knowing how environmental conditions cause changes in lifespan, reproductive mode and rate, and organismal health, and how these changes in life history shape individual and ecological outcomes.

Plasticity in response to environmental change may manifest both within and across generations. That is, the environment or physiology of a parent may affect the phenotype of its offspring without a change in genome. Our goals are to understand the molecular mechanisms, adaptive value, and evolutionary fitness consequences of within, inter-, and trans-generational plasticity in aging and life history strategy.

We use󾱴DzԳܲrotifers -- microscopic, aquatic, invertebrate animals, composed of about 1000 cells – as the experimental system for our work.These zooplankton have many advantages as a model system to study aging and phenotypic plasticity. Easy laboratory culture and a short, two-week lifespan allow longitudinal studies at high levels of individual-level replication. BecauseBrachionushas direct development without a larval stage, life table experiments include the entire lifespan, unlike in other invertebrate models. Asexual reproduction allows experimentation on isogenic lines, and inducible sexual reproduction permits outcrossing and genetics. Transparency enables imaging of cellular morphology and processes. Genome and transcriptome sequencing shows thatBrachionusrotifers have retained hundreds of human gene homologs that are absent from the genomes of established invertebrate models of aging. Thus, rotifers may be used to study many genes relevant to human aging that cannot be studied in other model systems.

Selected Publications

Liguori A., S. Korm, A. Profetto, E. Richters, and K.E. Gribble.2024.Intraspecific variability in maternal age effects on offspring lifespan and fecundity.Ecology and Evolution14:e11287.

Feng, H., G. Bavister, K.E. Gribble, and D.B. Mark Welch. 2023. Development of highly efficient CRISPR-mediated gene editing in the rotiferBrachionus manjavacas.PLoS Biology21(7): e3001888.

van Daalen, S.F., C.M. Hérnandez, H. Caswell, M.G. Neubert, K.E. Gribble. 2022. The contribution of maternal age heterogeneity to variance in lifetime reproductive output.The American Naturalist199(5):603-616

Gribble, K.E. 2021.Brachionusrotifers as a model for investigating dietary and metabolic regulators of aging.Nutrition and Healthy Aging6:1-15.

Hernández, C.M., S.F. van Daalen, H. Caswell, M.G. Neubert, K.E. Gribble. 2020. A demographic and evolutionary analysis of maternal effect senescence.Proceedings of the National Academy of Sciences, USA117(28):16431-16437.

Bock, M.J., G.C. Jarvis, E.L. Corey, E.E. Stone, K.E. Gribble. 2019.Maternal age alters offspring lifespan, fitness, and lifespan extension under caloric restriction.Scientific Reports9:3138.